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Medique Medi-Meclizine - 47682-479-33 - (MECLIZINE HYDROCHLORIDE)

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Drug Information of Medique Medi-Meclizine

Product NDC: 47682-479
Proprietary Name: Medique Medi-Meclizine
Non Proprietary Name: MECLIZINE HYDROCHLORIDE
Active Ingredient(s): 25    mg/1 & nbsp;   MECLIZINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Medique Medi-Meclizine

Product NDC: 47682-479
Labeler Name: Unifirst First Aid Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part336
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20081230

Package Information of Medique Medi-Meclizine

Package NDC: 47682-479-33
Package Description: 50 PACKET in 1 BOX, UNIT-DOSE (47682-479-33) > 2 TABLET, FILM COATED in 1 PACKET (47682-479-99)

NDC Information of Medique Medi-Meclizine

NDC Code 47682-479-33
Proprietary Name Medique Medi-Meclizine
Package Description 50 PACKET in 1 BOX, UNIT-DOSE (47682-479-33) > 2 TABLET, FILM COATED in 1 PACKET (47682-479-99)
Product NDC 47682-479
Product Type Name HUMAN OTC DRUG
Non Proprietary Name MECLIZINE HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20081230
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Unifirst First Aid Corporation
Substance Name MECLIZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Medique Medi-Meclizine


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